By Ramon Gil, M.D.
Whether or not your treating physician prescribed medication (s) for you at the time that you were diagnosed as having Parkinson’s Disease (PD), eventually, as the disease progresses, the problems associated with this condition will require “symptomatic treatment”. There are many different variables that one needs to consider to make the decision of which drug (s) to choose, but eventually, all patients with PD will require the use of levodopa, as monotherapy or in combination with other agents.
One of the disadvantages of levodopa is its short duration of effect. Because of this, multiple doses are required (anywhere from 3 to 6 times a day… sometimes more). This “pulsatile” stimulation of the dopamine receptors in the brain, along with progressive reduction in the production of dopamine in the brain (60 to 80% of the dopamine producing neurons are dead by the time the motor symptoms appear), are responsible factors for the so called: Motor Complications: Motor Fluctuations (MF) and Treatment Related Dyskinesias.
“Motor fluctuations” is the term used to describe the changes between akinetic (little or no movements), often called “Off states or periods” and mobile phases: “On states or periods”. This inability to control voluntary movements is confronted by a number of patients with PD as the disease progresses, and it is considered today as one of the most disabling problems associated with PD, becoming the number one reason for patients to seek for surgical treatment (Deep Brain Stimulation or DBS) as part of their remedy.
It is estimated that 30% of the patients with PD will develop MF within 2 years of being treated with levodopa, and practically all patients will by 10 years on levodopa therapy.
There are different types of “Off states”, the best and most often recognized are:
• End of dose deterioration
• Delayed onset of response
• Drug resistant “offs” (dose failure)
• Random “on-off” phenomenon, (unpredictable “off”)
• Freezing (unpredictable inability to initiate or finish a movement)
These are all very disabling and create a great deal of functional impairment, making the patient more dependent on the primary care giver, not to talk about the associated rise in the frequency of falls and subsequent increase in morbidity and mortality.
Two new formulations of levodopa recently approved and released, are longer acting, and have proven to improve this problem (Rytary® and Duopa®)
Dyskinesias (abnormal involuntary movements of the trunk, arms, legs, neck or even facial grimacing) are often physically and socially disabling.
There are three forms of dyskinesias seen in PD patients:
• Peak dose dyskinesias (twisting or dancing like movements affecting mainly the upper body, but could also involve the legs).
• Diphasic dyskinesias (involuntary movements involving the lower extremities).
• Off dystonias, also known as “Wearing off dystonias” (involuntary posturing of the distal part of the limbs frequently toes) associated with increased muscle tone, spasms and quite often pain.
It is known that 40% of patients with PD will experience dyskinesias after 1 year on levodopa therapy, and the number goes up to 50% within two years.
The graphic illustrates the problems confronted by PD patients in moderate to advance stages, to stay “On” with a good response to levodopa, no dyskinesias and short or minimal time “Off”. The higher the dose of levodopa, the more intense the dyskinesias may be. The lower the dose, the less or no dyskinesias they may experience, at the expense of increase amount of “Off” time. Adjustments in the doses of medications trying to optimize the motor control become very difficult, sometimes impossible to achieve. Understandably, many patients choose surgery (DBS) to correct or minimize this complicated problem.
Many people claim that “patients don’t mind dyskinesias as much as they mind being Off”. This is not entirely true. In a survey conducted by the National Parkinson Foundation, 56% of patients interviewed were embarrassed because of the dyskinesias, 52% believed that “others” were embarrassed (referring to relatives, friends, physicians and/or staff). A third admitted that they avoided social interaction because of the dyskinesias, 61% reported that the dyskinesias interfered with walking and 58% claimed that this problem interfered with sleeping.
Amantadine is the only medication available for the treatment of dyskinesias in PD. Common side effects include dizziness, lightheadedness due to low blood pressure upon standing (orthostatic hypotension), confusion, hallucinations, swelling in the feet/legs, weight gain, discoloration of the skin with a purplish mottled appearance (“livedo reticularis”). The recommended dose is 100 mg three times a day and it seems to help around 66% of the patients. A newer, once a day formulation of Amantadine is currently under development, and phase III clinical trials are being conducted as part of the process of FDA approval. The new formulation promises to be more effective and better tolerated. For more information please contact us at…..
Ramon A. Gil, M.D.
Medical Director, Parkinson’s Disease
Diplomate, American Board of Psychiatry and Neurology
Parkinson’s Disease Treatment Center of SW Florida